人工脊椎，棘突間隔/板
PMA 核准號：P110008 · 2026-05-22
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器材摘要
Prosthesis, spinous process spacer/plate is the device name listed in this FDA 510(k) record. The listed applicant is Companion Spine France. It received FDA 510(k) clearance on 2026-05-22. The device is classified under product code NQO. It was reviewed by the OR advisory panel. Product code NQO falls under the category of General Hospital, which covers general-purpose hospital equipment and supplies. Devices in this category are subject to specific FDA regulatory requirements.
常見問題
What is the Prosthesis, spinous process spacer/plate?
Prosthesis, spinous process spacer/plate is a medical device that received FDA 510(k) clearance on 2026-05-22. The listed applicant is Companion Spine France.
When did Prosthesis, spinous process spacer/plate receive FDA 510(k) clearance?
The clearance date for Prosthesis, spinous process spacer/plate can be found in the official FDA records.
Who is the listed applicant for Prosthesis, spinous process spacer/plate?
The FDA 510(k) record lists Companion Spine France as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prosthesis, spinous process spacer/plate?
The FDA product code for Prosthesis, spinous process spacer/plate is NQO. This falls under the General Hospital category.
相關臨床試驗
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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